| Primary Device ID | 00840479200194 |
| NIH Device Record Key | 81c9c210-249d-4fd5-9102-90e753a8d53a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FLOWTAIN LOW VISCOSITY PASTE |
| Version Model Number | 1FTLV |
| Company DUNS | 113170088 |
| Company Name | RELIANCE ORTHODONTIC PRODUCTS INC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840479200194 [Primary] |
| HIBCC | D7981FTLV0 [Previous] |
| EBF | Material, Tooth Shade, Resin |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-02-27 |
| Device Publish Date | 2026-02-19 |
| 00840479200279 - LIGHT BOND REGULAR PASTE | 2026-03-02 |
| 00840479200286 - LIGHT BOND REGULAR PASTE | 2026-03-02 |
| 00840479200293 - LIGHT BOND THIN PASTE | 2026-03-02 |
| 00840479200309 - LIGHT BOND THIN PASTE | 2026-03-02 |
| 00840479200316 - LIGHT CURE RETAINER | 2026-03-02 |
| 00840479200323 - LIGHT CURE RETAINER | 2026-03-02 |
| 00840479200330 - LUERLOK ULTRA BANDLOK | 2026-03-02 |
| 00840479200347 - LUERLOK ULTRA BANDLOK | 2026-03-02 |